FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DRAINOVAC COMPLETE CLOSED WOUND DRAINAGE DEVICE

K Number: K863482 · Decision Oct 14, 1986
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
23
Review Days
35

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Basic Information

Device Name
DRAINOVAC COMPLETE CLOSED WOUND DRAINAGE DEVICE
K Number
K863482
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cardio Metrics, Inc.
Date Received
September 9, 1986
Decision Date
October 14, 1986
Product Code
GCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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K961777 ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404
K955551 CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404
K954913 CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION)
K952562 CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE
K943022 CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRE
K940984 CARDIOMETRICS DUALFLOW SWITCH BOX
K933320 CARDIOMETRICS FLOMAP AND FLOMOD ULTRASOUND INSTRUMENT
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